SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6179021 | snp | A/G | 0.5 | 0 | intron-variant | Nfx1 | Mm_Celera | 4:40989625 | CACCAGCTCAGAGCG[A/G]ACACCCTGCTGAGCC | 74164 |
rs6194647 | snp | G/T | 0.5 | 0 | intron-variant | Nfx1 | Mm_Celera | 4:40990204 | ACGGACCACTCCTCT[G/T]CCCCCTGTCTTAGCA | 74164 |
rs6232057 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025480 | CTCTCTCGCCATGTT[C/G]ACAATGTGGGTCTAT | 74164 |
rs6232130 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025530 | CTAAGTCCTCTGTGG[C/T]TGGTAGAGACTCTCG | 74164 |
rs6232550 | snp | C/T | 0.156735 | 0.231952 | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025574 | ACTGGGTTGCTTTTT[C/T]CCTAGGCTTTCAGCA | 74164 |
rs6337282 | snp | C/T | 0.5 | 0 | intron-variant | Nfx1 | Mm_Celera | 4:40971236 | CGGGATGGGGAGGCT[C/T]GGCCCCTGGGTTTCC | 74164 |
rs6337798 | snp | C/G | 0.5 | 0 | intron-variant | Nfx1 | Mm_Celera | 4:40971296 | GGAGCGGACGTGGGC[C/G]TCNGGCGCCCCCCGC | 74164 |
rs6337800 | snp | C/T | 0.5 | 0 | intron-variant | Nfx1 | Mm_Celera | 4:40971299 | GCGGACGTGGGCNTC[C/T]GGCGCCCCCCGCGGG | 74164 |
rs6338334 | snp | C/T | 0.5 | 0 | intron-variant | Nfx1 | Mm_Celera | 4:40971385 | gggcggacggccggc[C/T]ggccgggcgTAGGCG | 74164 |
rs6339468 | snp | G/T | 0.5 | 0 | intron-variant | Nfx1 | Mm_Celera | 4:40971625 | AGACCCTCCCTGTTC[G/T]CTCCCTGATTGTTGG | 74164 |
rs6339947 | snp | C/T | 0.5 | 0 | intron-variant | Nfx1 | Mm_Celera | 4:40971704 | GACTGTTCGTATAAG[C/T]TATTTCCATTTTCTT | 74164 |
rs6339997 | snp | A/C | 0.5 | 0 | intron-variant | Nfx1 | Mm_Celera | 4:40971734 | TCAAGGTGTATTGGT[A/C]AATCCGGGCTTTCAA | 74164 |
rs13473226 | snp | A/G | | | synonymous-codon | Nfx1 | Mm_Celera | 4:40976762 | AACAAACCCGAGAGA[A/G]CACAGCCCTTCCGAG | 74164 |
rs27765445 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025679 | TTACGCCAAGCATCC[C/T]ACTGTAGGCCTTCTT | 74164 |
rs27765446 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025626 | TCTGAGCTCTGAACC[A/T]CTGTTCAAATATTCA | 74164 |
rs27765447 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025545 | TTGGTAGAGACTCTC[A/G]CATAGACAGCGGTAC | 74164 |
rs27765448 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025332 | TATCCAAAAGCTCCC[A/G]GATGTCTCTAGACTG | 74164 |
rs27765449 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41025208 | CCTAGCCATAGTCTG[A/G]TTGTCCCATTTGTTC | 74164 |
rs27765451 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Nfx1 | Mm_Celera | 4:41024913 | GAATGATTCTGTGTA[G/T]TGGAGGAGACTCATT | 74164 |
rs27765452 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41024701 | CATGGTGTCCAGTAC[A/G]CATTGACGGGGCATC | 74164 |
rs27765453 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41024610 | GCTTTCTCATTGAGC[C/T]TGTGCCGGCAGAGGA | 74164 |
rs27765454 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41024451 | GATTCTCTCATCTTA[G/T]CACTCTGCTTTACTC | 74164 |
rs27765455 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41024368 | GTGGGTGTGCTTGGC[A/G]GCAGTAGCGGCGATG | 74164 |
rs27765456 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Nfx1 | GRCm38.p3 | 4:41024190 | CGGTATGAGGAAGGG[A/C]CTGGAAGGACCTAGA | 74164 |
rs27765457 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nfx1 | Mm_Celera | 4:41024179 | AATGGAGGTGGCGGT[A/G]TGAGGAAGGGCCTGG | 74164 |
rs27765458 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41024107 | GGCTCTAATCATGGC[A/C]TGGTGGAGACAGAAA | 74164 |
rs27765459 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41024050 | AATGCCTGCTCCTCT[A/G]TGCTCCTGCACCTGT | 74164 |
rs27765460 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nfx1 | Mm_Celera | 4:41024043 | GGAGCAGAATGCCTG[C/T]TCCTCTGTGCTCCTG | 74164 |
rs27765461 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Nfx1 | Mm_Celera | 4:41023984 | ACCCAAGTCTCACAA[A/C]GGCCCCGATCCACGG | 74164 |
rs27765462 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41023563 | GAGGAGTCCTGAGCT[C/T]GTTCTGATCCCAGGG | 74164 |
rs27765463 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41023493 | CACAGACGCAAACAG[A/G]AAAGCATAAGTAAAA | 74164 |
rs27765464 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41023485 | AATAATGACACAGAC[A/G]CAAACAGGAAAGCAT | 74164 |
rs27765465 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Nfx1 | GRCm38.p3 | 4:41023454 | ACACCATCATCTGAC[C/G]CGCACAGTGCGCAGT | 74164 |
rs27765466 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nfx1 | Mm_Celera | 4:41023191 | AGTGGCTCTCAGGGC[C/T]GTATCTACCGATGGT | 74164 |
rs27765467 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Nfx1 | Mm_Celera | 4:41023150 | TACAGCTTTGGCTCC[G/T]TGTCCAGCCACTGGG | 74164 |
rs27786168 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nfx1 | Mm_Celera | 4:41022876 | GCTATGTATGGAGAA[A/G]TGATATAGTGACCTG | 74164 |
rs27786169 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41022246 | CCGAGTTAACCACTG[C/T]CTTCTCGTTTCAGGA | 74164 |
rs27786170 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41022177 | CAGTGTTGTCCTCTC[C/T]GTACTGTGTGGGCAG | 74164 |
rs27786171 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41022137 | GCTCCTGGTCTGGCA[A/G]CTCCTCTCTTCTGCA | 74164 |
rs27786172 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41022067 | CAAGGGCCATGAGGA[C/T]GAGCCACCACTCACC | 74164 |
rs27786173 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41021969 | TAAAGTAAGCTTATG[A/T]TGTAAGAAATGACGT | 74164 |
rs27786174 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41021941 | TGTGTGTTTCCCCCA[G/T]AATTAAGCCAGGTAA | 74164 |
rs27786175 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nfx1 | Mm_Celera | 4:41021870 | ACTGCTTATCCACCT[C/T]CCTAGCGGCAGCTGA | 74164 |
rs27786176 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41020897 | GAAGTTCTTGACTTA[C/T]GTAAAACTTATTCTG | 74164 |
rs27786177 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41019832 | TCTATTGTGTTTATG[C/T]GTCTGTGTGGATGTA | 74164 |
rs27786178 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41019156 | TGGTTTGGCTGCCTG[C/G]CAGTTTGTTTGTTTG | 74164 |
rs27786179 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41019063 | TCATTTACTGAGACA[A/G]AGGCCTTTCCTTACT | 74164 |
rs27786180 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41018838 | ACCTCACGTACATGC[A/G]GCCTGAGGCCCAGTC | 74164 |
rs27786181 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41018631 | GTCTGCACCTACACA[A/G]TGCAAGCCAGGGGTG | 74164 |
rs27786182 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Nfx1 | Mm_Celera | 4:41018475 | TGAGGAGTGTGCTGC[C/T]CTGGAAAGGAGAAAG | 74164 |
rs27786183 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41018326 | GTGAAGCCTGAGATA[C/G]GCATGCCCTCCTAAC | 74164 |
rs27786184 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Nfx1 | Mm_Celera | 4:41018224 | GCTTGACTCCCTATA[A/T]CCGGGAGGCCCTTGA | 74164 |
rs27786185 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41018208 | GAACCCACCAAGGAC[A/T]GCTTGACTCCCTATA | 74164 |
rs27786186 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nfx1 | Mm_Celera | 4:41018092 | ATTCTGGAAGTGTAC[A/G]CTGCTGCCTTCCAGC | 74164 |
rs27786187 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41017916 | AAGTGTCCGTATCCC[C/T]AGCACAGGGCGTCCT | 74164 |
rs27786188 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41017853 | TAAACATTAATAATA[C/G]GGTTTCCGAGGTCAC | 74164 |
rs27786189 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41017761 | TCTGGAGAGAGAAAG[G/T]CATGTTAACTCTTCT | 74164 |
rs27786190 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41017498 | ACCAGATGTGAAGGC[A/G]TGCTATGGCTATAGG | 74164 |
rs27786191 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41017445 | GATCTGAGTATAGAG[G/T]TGAACTGTTAGTGAA | 74164 |
rs27786192 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41017390 | CTGGTAGATATCCTT[A/G]TAGCCTCCCAAAGCC | 74164 |
rs27786193 | snp | A/C | 0.32 | 0.24 | intron-variant | Nfx1 | Mm_Celera | 4:41017158 | GTGGGCCCCACCAAC[A/C]CGTACATACATCATG | 74164 |
rs27786194 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41016259 | TGAATGTGCTGCCAC[G/T]GAGCTATGTCTCCAG | 74164 |
rs27786195 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41016250 | CTAAGCTAATGAATG[C/T]GCTGCCACTGAGCTA | 74164 |
rs27786196 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41016022 | AAAGTGAAGCCTGCC[G/T]GGCTGTCATGCAGTT | 74164 |
rs27786197 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41015901 | GCGCCTCCCAACGTG[C/T]CCATTGCTGTGCCCT | 74164 |
rs27786198 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Nfx1 | Mm_Celera | 4:41015782 | GGACCTGCGTCAGAT[A/C]TGTACACTGGATTCA | 74164 |
rs27786199 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41015655 | TCGGGTCATCAGGAC[A/C]ATGGTGTCATAGTTA | 74164 |
rs27786200 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41015461 | CCGCTGCTAGAGAGT[A/C]CAGAATTGACTTCAG | 74164 |
rs27786201 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Nfx1 | Mm_Celera | 4:41015214 | CTAGTTACGAAGCAA[C/T]ATCCCCTGTCACCTG | 74164 |
rs27786202 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41014783 | CCTCCAGGGCCACCC[A/G]TGATTGAATTGCTTG | 74164 |
rs27786203 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41014768 | ATGCATAGAATCAGG[A/C]CTCCAGGGCCACCCG | 74164 |
rs27786204 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41014519 | AAGCAGAGTTCCCAT[G/T]TGTCTTTCTTTCCTA | 74164 |
rs27786205 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41014447 | TAGTTACCTGGTCCC[A/G]TCTTACCCAGCTGAG | 74164 |
rs27786206 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nfx1 | Mm_Celera | 4:41014414 | CCGTCATGCTTACAG[C/T]ATTGTAAAAGTATTC | 74164 |
rs27786207 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41014349 | TTTGTAGGTGTATTT[C/T]GAAATTCAACCTACC | 74164 |
rs27786208 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41014316 | GGAGAGAGGGAAGTT[A/G]GAATGTTAAAGCAGG | 74164 |
rs27786209 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41014267 | ATCAGACTGGCTGAT[A/G]ATAAATCTCACCTCC | 74164 |
rs27786210 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41013845 | AGAAGCAGGTAATTT[C/T]TCAAGAAATAAAATG | 74164 |
rs27786211 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41013509 | AGAAGGCACCTCTGC[A/G]TCCAAAGCCACTGAG | 74164 |
rs27786212 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41013459 | AGATCTAATGATCAG[C/G]TGTGAGGCGTGAGAG | 74164 |
rs27786213 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41013321 | TGGATCAATCGTTCA[A/G]AGATGAGTGTGTTGT | 74164 |
rs27786214 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41013293 | TAGATGTGGGGTCAC[A/T]CCCCTGCCTTTATGG | 74164 |
rs27786215 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Nfx1 | Mm_Celera | 4:41012710 | AAAAAAGTGTTGTAT[A/T]ACCAGGGTTATGTGA | 74164 |
rs27786216 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nfx1 | Mm_Celera | 4:41010913 | GCCTGTAGCTTTGTG[C/T]ATGGAGAGCTGACAC | 74164 |
rs27786217 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41010778 | TTGCTGGGGATTAAA[A/C]CAAGGGCTTTGCACA | 74164 |
rs27786218 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nfx1 | Mm_Celera | 4:41009939 | CTGTCCTGGTGAACC[A/G]TGTCCCGGCCCCCAA | 74164 |
rs27786219 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41009917 | GGATGAGAGAGCAGT[A/G]TCTTCTCTGTCCTGG | 74164 |
rs27786220 | snp | A/T | 0.32 | 0.24 | intron-variant | Nfx1 | Mm_Celera | 4:41009891 | ATGCTGGGAGCTCAC[A/T]TGGGCCTTCTGGATG | 74164 |
rs27786221 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41009850 | TGATTACAGCCCAGA[A/G]ATTCAGCTGACGGCC | 74164 |
rs27786222 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41009401 | GAGCACCTTTTTCAC[C/T]TTAAATTAAGATTTG | 74164 |
rs27786223 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41009035 | ATTTCTCAGTCTCAA[A/G]TATAAAGCAAAATAG | 74164 |
rs27786224 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Nfx1 | Mm_Celera | 4:41008926 | CACACAGACCAAAAT[C/G]GCTCTCCTGAGAATG | 74164 |
rs27786225 | snp | A/G/T | 0.244898 | 0.249948 | intron-variant | Nfx1 | GRCm38.p3 | 4:41008859 | TAGAAGCATTTTACA[A/G/T]GGACTAGATGGTAGA | 74164 |
rs27786226 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41008559 | CTGAGGGACATTGGA[A/G]GCTCAGGATGGGATA | 74164 |
rs27786227 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41007411 | ATTTGAAATCACACT[G/T]CATTTTTCCCTGTAC | 74164 |
rs27786228 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nfx1 | Mm_Celera | 4:41007395 | TACCAGGCCAAAAAC[A/C]ATTTGAAATCACACT | 74164 |
rs27786229 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nfx1 | Mm_Celera | 4:41007066 | AACAGTAGTGTGACC[A/G]TTACATCAGTGGTTC | 74164 |
rs27786230 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nfx1 | Mm_Celera | 4:41005422 | TCTTGTCTTTCTTGT[C/T]TTTCACAGACTTCTG | 74164 |
rs27786231 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nfx1 | Mm_Celera | 4:41005064 | TAAGCCACATGGTGC[C/T]TCCTCAACAGTATGC | 74164 |
rs27786232 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nfx1 | Mm_Celera | 4:41004297 | AAAGTGGAGAAAAAT[A/G]GTGTTAACAGATAGA | 74164 |